Evidence map›Paper›PMID 38821492›Full record

ArticleBeneficial microbes2024

Gut microbiome and symptoms in females with irritable bowel syndrome: a cross-sectional analysis.

K J Kamp, A M Plantinga, K C Cain, R L Burr, C-S Tsai, Q Wu, S Y So, S Badu, T Savidge, R J Shulman and 1 more

Abstract read
In one paragraph

Article in Beneficial microbes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Altered molecular signature of the intestinal microbiota in irritable bowel syndrome patients versus healthy controls: An updated systematic review.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2026
    Pooled it
  2. Pooled it
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

K J Kamp16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.ORCID https://orcid.org/0000-0002-7753-3564
A M PlantingaWilliams College, Williamstown, MA, USA.ORCID https://orcid.org/0000-0001-6281-7727
K C Cain16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.ORCID https://orcid.org/0000-0002-5665-6952
R L Burr16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.
C-S Tsai16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.
Q WuBaylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
S Y SoBaylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
S BaduBaylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
T SavidgeBaylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
R J ShulmanBaylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.
M M Heitkemper16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.ORCID https://orcid.org/0000-0002-2938-1842

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Hashem B El-Serag · 2001 to 2026
$28.3M
Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogenP01AI152999 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HAAG, ANTHONY · 2020 to 2025
$12.0M
Decoding Antibiotic-induced Susceptibility to Clostridium difficile InfectionU01AI124290 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI BRITTON, ROBERT A, GAREY, KEVIN W · 2016 to 2020
$7.9M
PATHWAYS TO NEW BIOMARKERS IN RECURRENT ABDOMINAL PAIN IN CHILDRENR01NR013497 · NINR · BAYLOR COLLEGE OF MEDICINE · PI SAVIDGE, TOR C. · 2012 to 2024
$4.7M
A Prospective Study Examining the Role of Gestational SSRI Exposure in the Development of Functional Gastrointestinal DisordersR01DK130517 · NIDDK · NEW YORK UNIVERSITY · PI MARGOLIS, KARA GROSS, SAVIDGE, TOR C. · 2021 to 2024
$2.5M
Microbiome and Pain SupplementR01NR014479 · NINR · UNIVERSITY OF WASHINGTON · PI HEITKEMPER, MARGARET MCLEAN, SHULMAN, ROBERT J · 2014 to 2017
$1.8M
A Comprehensive Self-Management Intervention for individuals with Inflammatory Bowel DiseaseK23NR020044 · NINR · UNIVERSITY OF WASHINGTON · PI KAMP, KENDRA JOY · 2022 to 2024
$430k
NIAID NIH HHS P01 AI152999NIAID NIH HHS U01 AI124290NIDDK NIH HHS P30 DK056338NIDDK NIH HHS R01 DK130517NINR NIH HHS K23 NR020044NINR NIH HHS R01 NR013497NINR NIH HHS R01 NR014479
6 · The paper itself

Abstract

Irritable bowel syndrome (IBS), a disorder of gut-brain interaction, is associated with abdominal pain and stool frequency/character alterations that are linked to changes in microbiome composition. We tested whether taxa differentially abundant between females with IBS vs healthy control females (HC) are associated with daily gastrointestinal and psychological symptom severity. Participants (age 18-50 year) completed a 3-day food record and collected a stool sample during the follicular phase. They also completed a 28-day diary rating symptom intensity; analysis focused on the three days after the stool sample collection. 16S rRNA gene sequencing was used for bacterial identification. Taxon abundance was compared between IBS and HC using zero-inflated quantile analysis (ZINQ). We found that females with IBS (n = 67) had greater Bacteroides abundance (q = 0.003) and lower odds of Bifidobacterium presence (q = 0.036) compared to HC (n = 46) after adjusting for age, race, body mass index, fibre intake, and hormonal contraception use. Intestimonas, Oscillibacter, and Phascolarctobacterium were more often present and Christensenellaceae R-7 group, Collinsella, Coprococcus 2, Moryella, Prevotella 9, Ruminococcaceae UCG-002, Ruminococcaceae UCG-005, and Ruminococcaceae UCG-014 were less commonly present in IBS compared to HC. Despite multiple taxon differences in IBS vs HC, we found no significant associations between taxon presence or abundance and average daily symptom severity within the IBS group. This may indicate the need to account for interactions between microbiome, dietary intake, metabolites, and host factors.

Indexed as

BacteriaFecesGastrointestinal MicrobiomeIrritable Bowel SyndromeRNA, Ribosomal, 16SAdolescentAdultCross-Sectional StudiesFemaleHumansMiddle AgedYoung AdultRNA, Ribosomal, 16S

Identifiers

PMID38821492
PMCPMC12872350

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.